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1 polysome fractions and enhanced tolerance to begomovirus.
2 ern Asia is capable of interacting with a NW begomovirus.
3 he host range expansion of a host-restricted begomovirus.
4 related to DNA-A components of NW bipartite begomoviruses.
5 an intensively studied group of monopartite begomoviruses.
6 the components of the four cucurbit-adapted begomoviruses.
7 id relatives, and show GRDs are derived from begomoviruses.
8 d may have provided a selective advantage as begomoviruses adapted to a different environment and dif
10 ntinent was associated with several distinct begomoviruses along with a disease-specific betasatellit
13 er sequencing to confirm the identity of the begomoviruses and that all clones possessed a full compl
14 ism, we established a model system using two begomoviruses and their common host plant, Nicotiana ben
15 tes recombinant AL2/C2 proteins from several begomoviruses and to map the SnRK1 phosphorylation site
16 AL2 from Tomato golden mosaic virus (TGMV, a begomovirus) and to determine if the related L2 protein
17 first report of an indigenous NW monopartite begomovirus, and evidence is presented that it emerged f
18 o yellow leaf curl virus (TYLCV) and related begomoviruses are a major threat to tomato production wo
19 (known as betasatellites), the genomes of NW begomoviruses are exclusively bipartite and do not assoc
20 ed their closest nucleotide identities among begomoviruses, at approximately 90 and 81%, respectively
21 ine-109 in the AL2 proteins of two New World begomoviruses: Cabbage Leaf Curl Virus (CaLCuV) and Toma
24 maintenance of CLCuMuB by one of its cognate begomoviruses (cotton leaf curl Rajasthan virus) differs
25 n their patterns of variation and evolution, begomoviruses differ greatly from plant viruses with RNA
26 nuclear export of the bipartite geminivirus (Begomovirus) DNA genome was recently suggested by the fi
27 As a countermeasure, members of the genus Begomovirus (e.g., Cabbage leaf curl virus) encode an AL
28 AL2 protein encoded by members of the genus Begomovirus (e.g., Tomato golden mosaic virus) is a tran
32 tor protein) encoded by members of the genus Begomovirus has been shown to act as a silencing suppres
35 r efficient transreplication by a new helper begomovirus, including begomoviruses originating from th
36 Old World (OW) monopartite tomato-infecting begomoviruses, including lack of sap transmissibility, p
38 ence of B. tabaci-transmitted geminiviruses (begomoviruses), ipomoviruses, and torradoviruses has led
40 ult in co-infection of plants with different begomoviruses, leading to the appearance of further vari
41 analysis suggested that AL2 S109 evolved as begomoviruses migrated from the Old World to the New Wor
42 and was associated with a single recombinant begomovirus named Burewala strain of Cotton leaf curl Ko
43 RLK) identified as a virulence target of the begomovirus nuclear shuttle protein (NSP), leads to glob
44 mptoms when coinoculated with cassava mosaic begomoviruses onto a susceptible cultivar or a CMD2-resi
47 ism of transreplication of betasatellites by begomoviruses remains unknown, an analysis of betasatell
49 AL2 proteins of three subgroups of New World begomoviruses, resulting in a delay in viral DNA accumul
50 ian subcontinent and is associated with nine begomovirus species, whereas cassava brown streak diseas
51 sh that ToLDeV is an emergent NW monopartite begomovirus that is causing ToLCD in Ecuador and Peru.
53 e against the bipartite tomato severe rugose begomovirus, where a similar genome hypermethylation of
54 cterized whitefly-transmitted geminiviruses (begomoviruses) with origins in the New World (NW) have b
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